My Great Strides Story
Sue And Steve Liebler
Sue And Steve Liebler
As many of you know, our grandson Caden was born with cystic fibrosis. There is currently no cure and too many people with CF die young. Once again, we will be walking in the CF Foundation’s Great Strides on May 3rd to help change that reality.
CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure. Caden’s daily regimen includes pancreatic enzymes, nebulizer treatments and a special vibrating vest that helps loosen mucus in the chest and clear airways.
Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
Will you help us end cystic fibrosis?
By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.
CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure. Caden’s daily regimen includes pancreatic enzymes, nebulizer treatments and a special vibrating vest that helps loosen mucus in the chest and clear airways.
Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
Will you help us end cystic fibrosis?
By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.
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